17846-90-1

Basic information

• Product Name: Benzoic acid, 2-formyl-4,6-dimethoxy-, methyl ester
• CAS NO: 17846-90-1
• Molecular Formula: C11H12O5
• Molecular Weight: 224.213
• Mol File: 17846-90-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-formyl-4,6-dimethoxy-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-formyl-4,6-dimethoxy-, methyl ester(17846-90-1)
• EPA Substance Registry System: Benzoic acid, 2-formyl-4,6-dimethoxy-, methyl ester(17846-90-1)

Safety Data

• Hazardous Substances Data: 17846-90-1(Hazardous Substances Data)

Upstream product

• 142601-55-6 N,N-diethyl-2,4-dimethoxybenzamide 
• 868756-10-9 N,N-diethyl 2-formyl-4,6-dimethoxybenzamide 
• 17846-89-8 2-formyl-4,6-dimethoxy-benzoic acid 
• 74-88-4 methyl iodide 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 6110-37-8 methyl 2,4-dimethoxy-6-methylbenzoate 
• 3187-58-4 methyl orsellinate 
• 77-78-1 dimethyl sulfate 
• 3465-69-8 5,7-dimethoxyphthalide 
• 39828-35-8 2,4-dimethoxybenzoyl chloride 
• 21615-34-9 2-Methoxybenzoyl chloride 
• 53015-08-0 2-formyl-6-methoxy-benzoic acid 
• 85925-67-3 3-hydroxy-5,7-dimethoxy-(3H)-isobenzofuran-1-one 
• 579-75-9 2-Methoxybenzoic acid 

Downstream Products

• 17846-93-4 2-Propin-⁽¹⁾-yl-4.6-dimethoxy-benzoesaeure 
• 17846-92-3 cis-2-Propen-⁽¹⁾-yl-4.6-dimethoxy-benzoesaeuremethylester 
• 17947-63-6 2-Propin-⁽¹⁾-yl-4.6-dimethoxy-benzoesaeuremethylester 
• 1452584-43-8 C₁₈H₁₉NO₃ 
• 71030-11-0 beta-zearalenol 

Relevant articles and documents

Enantioselective total synthesis of β-zearalenol from (s)-propylene oxide

The total synthesis of 14-membered resorcylic acid macrolide, β-zearalenol, was accomplished starting from commercially available enantiomerically pure propylene oxide and methyl 2,4-dihydroxy-6-methylbenzoate using Grignard reaction, asymmetric dihydroxy

Probing the reactivity of o-phthalaldehydic acid/methyl ester: Synthesis of N-isoindolinones and 3-arylaminophthalides

A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was developed through aza-Wittig/cyclisation. The reaction of o-phthalaldehydic acid methyl ester with benzylic, aromatic and aliphatic azides gave N-isoindolinones w

Discovery of a potent and selective inhibitor for human carbonyl reductase 1 from propionate scanning applied to the macrolide zearalenone

In order to extend the chemical diversity available for organic polyketide synthesis, the concept of propionate scanning was developed. We observed that naturally occurring polyketides frequently comprise not only acetate, but also some propionate as buil